ABHD11 rabbit pAb - ES1570

ABHD11 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES1570-50, ES1570-100

Citations, Manuals and MSDS Available upon request.

Background: This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016],

Alternate Name: ABHD11; WBSCR21; PP1226; Abhydrolase domain-containing protein 11; Williams-Beuren syndrome chromosomal region 21 protein

Source: Rabbit

Applications: WB; ELISA

Dilution: Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.

Reactivity: Human; Rat; Mouse;

Immunogen: The antiserum was produced against synthesized peptide derived from human ABHD11. AA range:161-210

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Observed Band (KD): 32kD

Human Gene ID: 83451

Human SWISS Prot NO: Q8NFV4

Subcellular Location: mitochondrion,

Research Use Only